An assessment of sleep quality and sleep disordered breathing is determined from cardiopulmonary coupling between two physiological data series. An R-R interval series is derived from an electrocardiogram (ECG) signal. The normal beats from the R-R interval series are extracted to produce a normal-to-normal interval series. The amplitude variations in the QRS complex are used to extract a surrogate respiration signal (i.e., ECG-derived respiration) associated with the NN interval series. The two series are corrected to remove outliers, and resampled. The cross-spectral power and coherence of the two resampled signals are calculated over a plurality of coherence windows. For each coherence window, the product of the coherence and cross-spectral power is used to calculate coherent cross-power. Using the appropriate thresholds for the coherent cross-power, the proportion of sleep spent in CAP, non-CAP, and wake and/or REM are determined. Coherent cross-power can be applied to differentiate obstructive from non-obstructive disease, and admixtures of the same.
Legal claims defining the scope of protection, as filed with the USPTO.
1. A method of assessing sleep quality for a subject, wherein the method is performed in a computer-based system, comprising: deriving a heart rate interval series and a respiration series from at least one physiological signal obtained from the subject; calculating a measure of cardiopulmonary coupling, wherein the measure of cardiopulmonary coupling is computed based on the heart rate interval series and the respiration series; and automatically evaluating the spectral characteristics of the measure of cardiopulmonary coupling to differentiate between an obstructive sleep disorder and a non-obstructive sleep disorder.
2. The method according to claim 1 , wherein said evaluating step comprises: identifying at least one of a plurality of spectral peaks and broad coupling spectra to detect said obstructive sleep disorder.
3. The method according to claim 1 , wherein said evaluating step comprises: identifying at least one of a single dominant frequency and a narrow spectral dispersion to detect said non-obstructive sleep disorder.
4. The method according to claim 1 , wherein said evaluating step is independent of polysomnogram scoring.
5. The method according to claim 1 , further comprising: producing a graphical representation of said cardiopulmonary coupling.
6. The method according to claim 5 , further comprising: automatically evaluating said graphical representation to detect a CAP state, a non-CAP state, a wake state, or an REM state.
7. The method according to claim 5 , wherein 30-second epochs are applied to the graphical representation to thereby detect a CAP state, a non-CAP state, a wake state, or an REM state.
8. The method according to claim 5 further comprising: automatically evaluating the graphical representation of said cardiopulmonary coupling to detect at least one of an aging or pathological condition.
9. The method according to claim 1 , further comprising: automatically determining an effect of a drug or non-pharmacologic intervention.
10. The method according to claim 1 , further comprising: automatically determining an adverse or therapeutic effect of a drug or non-pharmacologic intervention.
11. The method according to claim 1 , wherein the respiration series is derived from an electrocardiogram signal.
12. The method according to claim 1 , wherein the heart rate series and the respiration series are each derived from different physiological signals.
13. The method according to claim 1 , wherein the physiological signal is obtained using an electrocardiogram.
Cooperative Patent Classification codes for this invention. Click any code to explore related patents in that topic.
July 12, 2005
June 8, 2010
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